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ARTHUR SMITH, MD

MD

Adult Medicine Physician

NPI: 1841359148Individual

Specialties, Licenses & Credentials

Adult Medicine PhysicianPrimary

Family Medicine — Adult Medicine

Code: 207QA0505X

MD013367E(PA)

Research & Publications (20)

Evolution of the total synthesis of (-)-okilactomycin exploiting a tandem oxy-cope rearrangement/oxidation, a Petasis-Ferrier union/rearrangement, and ring-closing metathesis.
PMID 19170499·J Am Chem Soc·2009
8-other
An efficient, second-generation synthesis of the signature dioxabicyclo[3.2.1]octane core of (+)-sorangicin A and elaboration of the (Z,Z,E)-triene acid system.
PMID 19182995·Org Lett·2009
8-other
Hemi-phorboxazole a: structure confirmation, analogue design and biological evaluation.
PMID 19637861·Org Lett·2009
8-other
Total synthesis of (+)-sorangicin A.
PMID 19663510·J Am Chem Soc·2009
8-other
(+)-Rimocidin synthetic studies: construction of the C(1-27) aglycone skeleton.
PMID 19621880·J Org Chem·2009
8-other
Total syntheses of the assigned structures of lituarines B and C.
PMID 18095694·J Am Chem Soc·2008
8-other
Synthesis and biological evaluation of phorboxazole congeners leading to the discovery and preparative-scale synthesis of (+)-chlorophorboxazole a possessing picomolar human solid tumor cell growth inhibitory activity.
PMID 18215059·J Org Chem·2008
8-other
Evolution of the Petasis-Ferrier union/rearrangement tactic: construction of architecturally complex natural products possessing the ubiquitous cis-2,6-substituted tetrahydropyran structural element.
PMID 18489082·Acc Chem Res·2008
8-other
Total synthesis of (+)-psymberin (irciniastatin A): catalytic reagent control as the strategic cornerstone.
PMID 19072197·Org Lett·2008
7-preclinical
Gram-scale synthesis of (+)-spongistatin 1: development of an improved, scalable synthesis of the F-ring subunit, fragment union, and final elaboration.
PMID 18754594·Org Lett·2008
8-other
A second-generation total synthesis of (+)-phorboxazole A.
PMID 18215058·J Org Chem·2008
8-other
Total synthesis of (-)-aplaminal.
PMID 18754624·Org Lett·2008
8-other
Ortho-TMS benzaldehyde: an effective linchpin for type II anion relay chemistry (ARC).
PMID 18666303·Angew Chem Int Ed Engl·2008
8-other
Total synthesis of (-)-2-epi-peloruside A.
PMID 19007239·Org Lett·2008
7-preclinical
Evolution of multi-component anion relay chemistry (ARC): construction of architecturally complex natural and unnatural products.
PMID 19030533·Chem Commun (Camb)·2008
6-review
Total synthesis of (-)-okilactomycin.
PMID 17997560·J Am Chem Soc·2007
8-other
Total synthesis of (+)-tedanolide.
PMID 17691787·J Am Chem Soc·2007
7-preclinical
Syntheses of (-)-oleocanthal, a natural NSAID found in extra virgin olive oil, the (-)-deacetoxy-oleuropein aglycone, and related analogues.
PMID 17685574·J Org Chem·2007
8-other
The spirastrellolides: construction of the southern C(1)-C(25) fragment exploiting anion relay chemistry.
PMID 17637031·Org Lett·2007
7-preclinical
Anion relay chemistry extended. Synthesis of a gorgonian sesquiterpene.
PMID 17637030·Org Lett·2007
8-other

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

Contact & Hours

Address
535 PINE ST
PHILADELPHIA, PA 19106

Location

Practice Location

535 PINE ST, PHILADELPHIA, PA
(215) 922-5180

Quick Facts

NPI
1841359148
Entity Type
Individual
Gender
Male
Medicare
Not confirmed
Specialties
1
Locations
1
Publications
20

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